3-Methoxyphenethylamine

97%

  • Product Code: 72188
  Alias:    2-(3-Methoxyphenyl)ethylamine; m-methoxyphenylethylamine
  CAS:    2039-67-0
Molecular Weight: 151.21 g./mol Molecular Formula: C₉H₁₃NO
EC Number: 218-017-9 MDL Number: MFCD00008187
Melting Point: Boiling Point: 118-119 °C6 mm Hg(lit.)
Density: 1.038 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its structure makes it suitable for the development of compounds targeting the central nervous system, particularly in the synthesis of potential psychotropic agents. Additionally, it has been explored in research settings for its role in studying neurotransmitter analogs, aiding in the understanding of neurological processes and the development of therapeutic drugs. Its methoxy and phenethylamine groups contribute to its versatility in chemical reactions, enabling the creation of diverse derivatives with potential applications in medicinal chemistry.
Product Specification:
Test Specification
PurityGC 96.5 100%
PURITYNONAQUEOUS TITRATION 96.5 100%
REFRACTIVE INDEX N20D 1.537-1.541
APPEARANCE Colorless to yellow liquid
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $13.37
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5.000 10-20 days $25.56
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25.000 10-20 days $82.58
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100.000 10-20 days $306.74
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500.000 10-20 days $1,208.88
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3-Methoxyphenethylamine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its structure makes it suitable for the development of compounds targeting the central nervous system, particularly in the synthesis of potential psychotropic agents. Additionally, it has been explored in research settings for its role in studying neurotransmitter analogs, aiding in the understanding of neurological processes and the development of therapeutic drugs. Its methoxy and phenethylamine groups contribute to its versatility in chemical reactions, enabling the creation of diverse derivatives with potential applications in medicinal chemistry.
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